makeO toothsi
Numbers are the ones on makeO toothsi's own site, read Nov 13, 2026. WhatsApp opens your own chat with a first line you can change that names this site; nothing you write reaches us.
makeO toothsi is one of India's largest at-home clear aligner brands, launched in 2018 by a team of orthodontists and now run under the makeO umbrella. It uses a hybrid model: a technician performs a 3D scan (at the patient's home or in a partner clinic), aligners are mail-delivered, and progress is remotely monitored by makeO's own dentists, with optional in-clinic care. It sells three tiers (Classic, Ace, Luxe) from Rs 52,999 with EMI financing and a smile guarantee. Sources
Sourced from each brand's published terms and primary FDA device records. Prices checked against their sources Nov 11, 2026, FDA records read Nov 10, 2026. How we verify. Not dental or medical advice.
At a glance
Prices verified Nov 11, 2026makeO toothsi (makeO toothsi clear aligners) is a clear aligner brand available to new patients that has no FDA device recall on file. Treatment is hybrid (remote care with an in-person clinic option).
- Treatment length
- 8-12 monthstypical
- Supervision
- Hybrid
- FDA safety
- No recalls
- Starting price
What it can treat
In makeO toothsi's own words: Crowding; Spacing and gaps; Complex / comprehensive cases (per provider). Sources
Custom clear aligner trays set up from a scan taken in-clinic or via an at-home kit, then worn at home under clinician oversight. Each set is worn Standard clear-aligner wear of 20 to 22 hrs/day, trays changed per the treatment plan (exact interval not published by the brand), moving teeth incrementally. Material: Classic tier: made-in-India PETG; Ace and Luxe tiers: German-made triple-ply (imported). Sources
Safety & recalls
This brand's FDA device record under the aligner product code NXC: recalls and MAUDE adverse-event reports, verified Nov 10, 2026.
A raw count of unverified FDA reports filed under “makeO toothsi” and product code NXC, not a rate. None on file may reflect how new or small the brand is, not proof of safety. Every brand's count is on the safety board.
Read from the FDA's database every day, last on Nov 10, 2026. Unchanged since we first recorded it on Sep 30, 2026.
How treatment is supervised
Remote care day to day, with a clinic scan or check-up available when you want one. Suits: at-home convenience with a clinician you can see in person.
makeO toothsi: Remote monitoring plus virtual dentist/orthodontist consultations by makeO's in-house clinicians; in-clinic support optional Sources
Brand specs
- Whitening
- Luxe: free professional whitening (advertised Rs 12,000 value); Classic and Ace: paid add-on
- Refinements / touch-ups
- Classic: up to 3 sets; Ace: up to 10 sets; Luxe: unlimited refinements
- Clinical oversight
- Remote monitoring plus virtual dentist/orthodontist consultations by makeO's in-house clinicians; in-clinic support optional
- Headquarters
- Mumbai, India
Clear aligners are FDA Class II devices (product code NXC, 21 CFR 872.5470), cleared through the 510(k) process. makeO toothsi treatment is hybrid (remote care with an in-person clinic option).
Where the makeO toothsi facts come from
The pages behind this brand's profile, specs and supervision model. Prices, treatment length and FDA records each link to their own source where they appear.
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Safety notices for at-home aligners
Regulatory safety findings a current reference should carry, even when the live per-brand feed has not caught up. Each is cited and dated.
Dental bodies caution against straightening teeth without an in-person exam
The American Dental Association maintains a standing policy discouraging direct-to-consumer teeth straightening, reaffirmed in December 2023 on patient-safety grounds. The American Association of Orthodontists holds that treatment should be under the in-person supervision of a licensed orthodontist, warns that moving teeth without an exam and X-rays can miss gum disease or cavities and cause irreversible, expensive harm (bone and tooth loss, receding gums, changed bites), and urges patients to report problems to the FDA. See a dentist before starting, and stop and seek care if you notice pain, looseness, or bleeding.
American Dental Association; American Association of Orthodontists · as of Dec 1, 2023
Reported harms in the FDA device adverse-event database
Thousands of adverse-event reports have been filed with the FDA under the sequential clear-aligner product code (NXC), the large majority coded as injuries, spanning both in-office and at-home brands. A peer-reviewed analysis of the NXC reports filed from 2010 to 2020 (651 reports, 104 of them involving direct-to-consumer aligners) found the direct-to-consumer reports dominated by bite problems (41.3%), orofacial pain (29.8%) and periodontal harm (26.6%) such as loose teeth, gum recession and bone loss, with tooth sensitivity, jaw (TMJ) problems, fractured teeth and tooth loss also reported; the authors note that some of these harms are irreversible. These are unverified spontaneous reports, not incidence rates, and do not establish that any device caused the event, but they underline why an in-person check and professional oversight matter.
Belgal et al., Dentistry Journal 2023 (analysis of FDA MAUDE reports, product code NXC) · as of Sep 30, 2026
Ways to start makeO toothsi
Every way to start, lowest price first.
makeO toothsi has 3 tracked ways to start; its plans are priced differently (some state no monthly figure), so each is shown with its own source below rather than ranked.
Prices are each brand's stated starting figure, not the total cost. They change often; each links to its source. Re-verified 2026-11-11. This is information, not dental or medical advice.
Clinical evidence & professional guidance
No registered study names makeO toothsi
Independent clinical evidence on individual aligner brands is limited, and both the American Dental Association and the American Association of Orthodontists advise an in-person exam and dentist or orthodontist supervision before treatment. The clear aligner studies we index cover the category as a whole (134 registered on ClinicalTrials.gov).